Primary Site >> Stomach Cancer
Gene >> NRCAM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108191747:108191747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139663718 |
| CDS Mutation | c.1885G>A |
| AA Mutation | p.Ala629Thr(p.A629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108180384:108180384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151029926 |
| CDS Mutation | c.2690G>A |
| AA Mutation | p.Arg897His(p.R897H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108232368:108232368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763460173 |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Cys(p.R129C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108198088:108198088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1219G>A |
| AA Mutation | p.Asp407Asn(p.D407N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108191807:108191807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565277285 |
| CDS Mutation | c.1825G>A |
| AA Mutation | p.Asp609Asn(p.D609N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108181881:108181881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768851472 |
| CDS Mutation | c.2587G>A |
| AA Mutation | p.Glu863Lys(p.E863K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108194044:108194044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751996742 |
| CDS Mutation | c.1758G>T |
| AA Mutation | p.Arg586Ser(p.R586S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108240024:108240024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.41C>T |
| AA Mutation | p.Ala14Val(p.A14V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108184484:108184484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2166G>T |
| AA Mutation | p.Met722Ile(p.M722I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108168309:108168309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3281T>C |
| AA Mutation | p.Val1094Ala(p.V1094A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108232366:108232366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770132892 |
| CDS Mutation | c.387C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108184532:108184532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2118A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108178030:108178030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576153014 |
| CDS Mutation | c.2934G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108166946:108166946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3441A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108191760:108191760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139719404 |
| CDS Mutation | c.1872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |